Department of Neurosurgery, NYU Langone Medical Center, New York, New York, USA.
Department of Neurosurgery, NYU Langone Medical Center, New York, New York, USA.
World Neurosurg. 2020 Jan;133:318-323. doi: 10.1016/j.wneu.2019.08.099. Epub 2019 Aug 23.
Idiopathic spinal cord herniation is a disorder in which the spinal cord herniates through a dural defect. We present a case in which both the standard surgical method and a salvage method failed.
A 36-year-old man presented with 2 years of progressive numbness and proximal hip flexion weakness of both lower extremities. Magnetic resonance imaging of the thoracic spine was suggestive for a ventral spinal cord herniation at the T6/7 level. He was initially treated with reduction of his cord herniation, placement of a ventral sling of collagen matrix over the dural defect to prevent re-herniation, with a laminoplasty. He developed a blood-pressure-dependent paraparesis that did not recover despite a return to the operating room (OR) for removal of the laminoplastic bone flap. He was again taken to the OR, the sling was removed and we enlarged the ventral dural defect rostrally and caudally to prevent strangulation of the hernia as described by Watanabe. Though in the short term he was able to recover and transfer to physical therapy, after going home he developed lower extremity weakness and low-pressure headaches. Magnetic resonance imaging showed a ventral epidural cerebrospinal fluid pocket retropulsing the spinal cord, as well as pockets of ventral cerebrospinal fluid collections remote from the surgery site. The patient returned to the OR and the initial surgery with the ventral sling was re-performed with resolution of the headaches; the patient was neurologically stable and transferred to rehabilitation. Long-term he developed left intercostal pain at the level of the surgery without radiological correlate.
In this patient there was no single satisfactory surgical treatment of his ventrally herniated spinal cord-partly related to the herniated component of the cord acting as a mass within a narrow canal at the apex of the thoracic kyphosis. We encountered previously unreported complications of the ventral defect widening technique of surgical treatment.
特发性脊髓疝是一种脊髓通过硬脑膜缺陷疝出的疾病。我们报告了一例标准手术方法和挽救方法均失败的病例。
一名 36 岁男性,出现进行性下肢麻木和双侧下肢近端髋关节屈曲无力 2 年。胸椎磁共振成像提示 T6/7 水平有脊髓腹侧疝。他最初接受了脊髓疝复位治疗,在硬脑膜缺损处放置胶原基质腹侧吊带以防止再次疝出,并进行了椎板成形术。他出现了血压依赖性截瘫,尽管返回手术室(OR)移除椎板成形术的骨瓣,但截瘫仍未恢复。他再次被送往 OR,移除了吊带,并扩大了腹侧硬脑膜缺损的头侧和尾侧,以防止像 Watanabe 描述的那样疝出物的绞窄。尽管他在短期内能够恢复并转移到物理治疗,但回家后他出现了下肢无力和低压性头痛。磁共振成像显示脊髓腹侧硬膜外脑脊液口袋向后推压脊髓,以及远离手术部位的腹侧脑脊液口袋。患者返回 OR,再次进行了带有腹侧吊带的初始手术,头痛得到缓解;患者神经功能稳定,并转移到康复科。长期以来,他在手术部位出现左侧肋间疼痛,但无影像学相关表现。
在本例患者中,没有一种单一的手术方法可以满意地治疗其腹侧疝出的脊髓——部分原因是疝出的脊髓部分在胸椎后凸顶点的狭窄管腔内充当了一个肿块。我们遇到了以前未报道过的腹侧缺陷扩大技术治疗的并发症。